Pomorzanka, Ul

4 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• UNSAFE COL2 refused lines

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

• COLOR LBLG1 refused line

  Artificial coloring not declared

  The product appeared to contain an artificial coloring without labeling that states that fact.

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• STD IDENT1 refused line

  Does not conform to standard of identity

  The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.

Questions about Pomorzanka, Ul

Is Pomorzanka, Ul on an FDA import alert?

Yes. As of October 25, 2026, Pomorzanka, Ul is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for makarena fruit jelly; FDA published the listing on June 24, 2016.

Has FDA refused shipments from Pomorzanka, Ul?

Yes. FDA refused 2 shipment lines from Pomorzanka, Ul between November 12, 2019 and February 8, 2022. The most recent, on February 8, 2022, was candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Pomorzanka, Ul's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 2 lines) and COLOR LBLG (artificial coloring not declared, 1 line).

What is Pomorzanka, Ul's FEI number?

Pomorzanka, Ul's FDA Establishment Identifier (FEI) is 3010741285.

Can shipments from Pomorzanka, Ul still enter the U.S.?

Shipments of makarena fruit jelly from Pomorzanka, Ul can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).